Erschienen in:
17.06.2016 | Original Article
Light transmittance and polymerization kinetics of amorphous calcium phosphate composites
verfasst von:
Matej Par, Danijela Marovic, Hrvoje Skenderovic, Ozren Gamulin, Eva Klaric, Zrinka Tarle
Erschienen in:
Clinical Oral Investigations
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Ausgabe 4/2017
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Abstract
Objectives
This study investigated light transmittance and polymerization kinetics of experimental remineralizing composite materials based on amorphous calcium phosphate (ACP), reinforced with inert fillers.
Materials and methods
Light-curable composites were composed of Bis-EMA-TEGDMA-HEMA resin and ACP, barium glass, and silica fillers. Additionally, a commercial composite Tetric EvoCeram was used as a reference. Light transmittance was recorded in real-time during curing, and transmittance curves were used to assess polymerization kinetics. To obtain additional information on polymerization kinetics, temperature rise was monitored in real-time during curing and degree of conversion was measured immediately and 24 h post-cure.
Results
Light transmittance values of 2-mm thick samples of uncured ACP composites (2.3–2.9 %) were significantly lower than those of the commercial composite (3.8 %). The ACP composites presented a considerable transmittance rise during curing, resulting in post-cure transmittance values similar to or higher than those of the commercial composite (5.5–7.9 vs. 5.4 %). The initial part of light transmittance curves of experimental composites showed a linear rise that lasted for 7–20 s. Linear fitting was performed to obtain a function whose slope was assessed as a measure of polymerization rate. Comparison of transmittance and temperature curves showed that the linear transmittance rise lasted throughout the most part of the pre-vitrification period.
Conclusions
The linear rise of light transmittance during curing has not been reported in previous studies and may indicate a unique kinetic behavior, characterized by a long period of nearly constant polymerization rate.
Clinical relevance
The observed kinetic behavior may result in slower development of polymerization shrinkage stress but also inferior mechanical properties.